Mutation of solute carrier SLC16A12 associates with a syndrome combining juvenile cataract with microcornea and renal glucosuria (Q28270419)

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Mutation of solute carrier SLC16A12 associates with a syndrome combining juvenile cataract with microcornea and renal glucosuria
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    Mutation of solute carrier SLC16A12 associates with a syndrome combining juvenile cataract with microcornea and renal glucosuria (English)
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    Barbara Kloeckener-Gruissem
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    Kristof Vandekerckhove
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    Gudrun Nürnberg
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    John Neidhardt
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    Christina Zeitz
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    Peter Nürnberg
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    Isaak Schipper
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    Wolfgang Berger
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    March 2008
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    82
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    3
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    772-9
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